Query author contributions in Reactome

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Details on Person Corydon, TJ

Class:Id	Person:70804
_displayName	Corydon, TJ
_timestamp	0000-00-00 00:00:00
firstname	Thomas J
initial	TJ
surname	Corydon
(author)	[LiteratureReference:70801] Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism [LiteratureReference:70864] Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans [LiteratureReference:5621453] Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis [LiteratureReference:9650573] Dominant-negative SERPING1 variants cause intracellular retention of C1 inhibitor in hereditary angioedema
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No pathways have been reviewed or authored by Corydon, TJ (70804)